A sequential anionic [4 + 2] cycloaddition and thermal [4 + 2] cycloreversion strategy to furocoumarins : A concise synthesis of methoxsalen
- 19 December 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (51) , 9617-9618
- https://doi.org/10.1016/0040-4039(94)88526-5
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Synthesis and photooxygenation of the 2H-4,8,9-trimethylfuro[2',3':5,6]naphtho[1,2-b]pyran-2-one, an unnatural furocoumarin with a benzene spacerThe Journal of Organic Chemistry, 1993
- Synthesis of psoralens and analoguesJournal of Photochemistry and Photobiology B: Biology, 1992
- Novel bicycloannulation via tandem vinylation and intramolecular Diels-Alder reaction of five-membered heterocycles: a new approach to construction of psoralen and azapsoralenJournal of the American Chemical Society, 1984
- A new synthesis of methoxalenJournal of Heterocyclic Chemistry, 1980
- New synthetic methods for the regioselective annelation of aromatic rings: 1-hydroxy-2,3-disubstituted naphthalenes and 1,4-dihydroxy-2,3-disubstituted naphthalenesThe Journal of Organic Chemistry, 1978